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Human Mutation, ISSN 1059-7794, 06/2012, Volume 33, Issue 6, pp. 981 - 988
Journal Article
Human Mutation, ISSN 1059-7794, 08/2013, Volume 34, Issue 8, pp. 1111 - 1118
Journal Article
Cochrane database of systematic reviews (Online), ISSN 1469-493X, 2008, Issue 3, p. CD004159
Journal Article
Journal of Neurology, Neurosurgery & Psychiatry, ISSN 0022-3050, 12/1998, Volume 65, Issue 6, pp. 881 - 889
OBJECTIVES To determine the prevalence and nature of global cognitive dysfunction and language deficits in an unselected population based cohort of patients... 
Aphasia | Motor neuron disease | Dementia | PRESENILE-DEMENTIA | SURGERY | aphasia | motor neuron disease | PSYCHIATRY | PALSY | POSITRON EMISSION TOMOGRAPHY | dementia | AMYOTROPHIC-LATERAL-SCLEROSIS | HUNTINGTONS-DISEASE | ALZHEIMERS | CLINICAL NEUROLOGY | Studies | Neurology | Amyotrophic lateral sclerosis | Language | Speech disorders
Journal Article
BMJ Case Reports, ISSN 1757-790X, 2010, Volume 2010, Issue feb02 1, pp. bcr1020092380 - bcr1020092380
Following an episode of syncope, a 42-year-old woman was referred to exclude a cardiac cause. This primary event was determined to be a straightforward case of... 
Trauma | Vertigo | Head injuries
Journal Article
Trends in Neurosciences, ISSN 0166-2236, 01/1999, Volume 22, Issue 1, pp. 44 - 45
Journal Article
Journal Article
Molecular Genetics and Metabolism, ISSN 1096-7192, 12/2001, Volume 74, Issue 4, pp. 458 - 475
Journal Article
Medicine, ISSN 1357-3039, 2004, Volume 32, Issue 11, pp. 119 - 123
Muscle disorders may be determined genetically or may be acquired and can present at any age. They can be classified in terms of causative genetic mutations,... 
acquired myopathy | metabolic myopathy | muscular dystrophy | muscle ion channel disorders | nerve | muscle | spinal cord | inflammatory myopathy | neurology | congenital myopathy
Journal Article
Journal of Neuroscience, ISSN 0270-6474, 05/2002, Volume 22, Issue 10, pp. 3953 - 3962
The mechanisms by which trophic factors bring about spinal motor neuron (MN) survival and regulate their number during development are not well understood. We... 
Bax | Neuronal death | Organotypic | Subpopulation | Trophic factor | Apoptosis | GDNF FAMILY | NEURTURIN RECEPTOR | trophic factor | SYMPATHETIC NEURONS | apoptosis | DEATH | organotypic | NEUROSCIENCES | CEREBRAL-CORTEX | NERVE GROWTH-FACTOR | RETINAL GANGLION-CELLS | FACTOR DEPRIVATION | subpopulation | neuronal death | BAX-DEFICIENT MICE | MOTONEURONS | Brain-Derived Neurotrophic Factor - pharmacology | Cyclic AMP - analogs & derivatives | Mice, Mutant Strains | Glial Cell Line-Derived Neurotrophic Factor | Motor Neurons - cytology | Nerve Tissue Proteins - pharmacology | Proto-Oncogene Proteins c-ret | Spinal Cord - cytology | Culture Media, Serum-Free - pharmacology | Ciliary Neurotrophic Factor - pharmacology | Cell Survival - physiology | Motor Neurons - drug effects | Animals, Newborn | Proto-Oncogene Proteins - metabolism | Cell Survival - drug effects | Drosophila Proteins | Motor Neurons - physiology | Receptor Protein-Tyrosine Kinases - deficiency | Mice, Inbred C57BL | Proto-Oncogene Proteins - deficiency | Thionucleotides - pharmacology | bcl-2-Associated X Protein | Receptor Protein-Tyrosine Kinases - metabolism | Mice, Inbred C3H | Cyclic AMP - pharmacology | Homozygote | Animals | Glial Cell Line-Derived Neurotrophic Factor Receptors | Nerve Growth Factors | Spinal Cord - physiology | Mice | Proto-Oncogene Proteins c-bcl-2 | In Vitro Techniques
Journal Article